BARISANI, DONATELLA
BARISANI, DONATELLA
DIPARTIMENTO DI MEDICINA E CHIRURGIA (SCHOOL OF MEDICINE AND SURGERY)
Saturability of hepatic iron deposits in genetic hemochromatosis
1992 Mandelli, C; Cesarini, L; Piperno, A; Fargion, S; Fracanzani, A; Barisani, D; Conte, D
Transferrin receptor 1 (TfR1) and putative stimulator of Fe transport (SFT) expression in iron deficiency and overload: An overview
2002 Barisani, D; Conte, D
A new human cell line, PDSS-26, from poorly differentiated synovial sarcoma, with unique chromosomal anomalies
2003 Berardi, A; Parafioriti, A; Barisani, D; Papp, B; Armiraglio, E; Martinoli, M; Dalpra', L; Santoro, A
Adaptive changes of duodenal iron transport proteins in celiac disease
2004 Barisani, D; Parafioriti, A; Bardella, M; Zoller, H; Conte, D; Armiraglio, E; Trovato, C; Koch, R; Weiss, G
Hemochromatosis gene mutations and iron metabolism in celiac disease
2004 Barisani, D; Ceroni, S; Del Bianco, S; Meneveri, R; Bardella, M
IL-10 polymorphisms are associated with early-onset celiac disease and severe mucosal damage in patients of caucasian origin
2006 Barisani, D; Ceroni, S; Meneveri, R; Cesana, B; Bardella, M
Usefulness of the organ culture system in the in vitro diagnosis of coeliac disease: a multicentre study
2006 Picarelli, A; Di Tola, M; Sabbatella, L; Anania, M; Calabrò, A; Renzi, D; Bai, J; Sugai, E; Carroccio, A; Di Prima, L; Bardella, M; Barisani, D; Ribes Koninckx, C; Aliaga, E; Gasparin, M; Bravi, E; Multicentre Organ Culture System Study, G
Clinical and genetic familial study of 61 children showing different epileptic phenotypes.
2007 Combi, R; Redaelli, S; Grioni, D; Contri, M; Barisani, D; Lavitrano, M; Tredici, G; Tenchini, M; Bertolini, M; Dalpra', L
Lack of haptoglobin affects iron transport across duodenum by modulating ferroportin expression
2007 Marro, S; Barisani, D; Chiabrando, D; Fagoonee, S; Muckenthaler, M; Stolte, J; Meneveri, R; Haile, D; Silengo, L; Altruda, F; Tolosano, E
CD34 human hematopoietic progenitor cell line, MUTZ-3, differentiates into functional osteoclasts
2007 Ciraci, E; Barisani, D; Parafioriti, A; Formisano, G; Arancia, G; Bottazzo, G; Berardi, A
Endometrioid-like yolk sac and Sertoli-Leydig cell tumors in the same subject carrier of a Y heterochromatin insertion into 1qh region: casual or causal association?
2007 Sala, E; Villa, N; Crosti, F; Miozzo, M; Perego, P; Cappellini, A; Bonazzi, C; Barisani, D; Dalpra', L
Morphologic Overlap between Infantile Myofibromatosis and Infantile Fibrosarcoma: A Pitfall in Diagnosis
2008 Alaggio, R; Barisani, D; Ninfo, V; Rosolen, A; Coffin, C
Hepcidin and iron-related gene expression in subjects with Dysmetabolic Hepatic Iron Overload
2008 Barisani, D; Pelucchi, S; Mariani, R; Galimberti, S; Trombini, P; Fumagalli, D; Meneveri, R; Nemeth, E; Ganz, T; Piperno, A
Retinoic acid- and phorbol ester-induced neuronal differentiation down-regulates caveolin expression in GnRH neurons
2008 D'Orlando, C; Guzzi, F; Gravati, M; Biella, G; Toselli, M; Meneveri, R; Barisani, D; Parenti, M
Expression of hepcidin and other iron-related genes in type 3 hemochromatosis due to a novel mutation in transferrin receptor-2.
2009 Pelucchi, S; Mariani, R; Trombini, P; Coletti, S; Pozzi, M; Paolini, V; Barisani, D; Piperno, A
Clinical and genetic familial study of a large cohort of Italian children with idiopathic epilepsy
2009 Combi, R; Grioni, D; Contri, M; Redaelli, S; Redaelli, F; Bassi, M; Barisani, D; Lavitrano, M; Tredici, G; Tenchini, M; Bertolini, M; Dalpra', L
Celiac disease: from pathogenesis to novel therapies
2009 Schuppan, D; Junker, Y; Barisani, D
Analysis of HLA and Non-HLA Alleles Can Identify Individuals at High Risk for Celiac Disease
2009 Romanos, J; van Diemen, C; Nolte, I; Trynka, G; Zhernakova, A; Fu, J; Bardella, M; Barisani, D; Mcmanus, R; van Heel, D; Wijmenga, C
Increased p21 expression in chondrocytes of achondroplasic children independently from the presence of the G380R FGFR3 mutation
2009 Parafioriti, A; del Bianco, S; Barisani, D; Armiraglio, E; Peretti, G; Albisetti, W
Six new coeliac disease loci replicated in an Italian population confirm association with coeliac disease
2009 Romanos, J; Barisani, D; Trynka, G; Zhernakova, A; Bardella, M; Wijmenga, C